Literature DB >> 2804986

Phase I clinical trial of interleukin 2 and alpha-interferon: toxicity and immunologic effects.

G T Budd1, B Osgood, B Barna, J M Boyett, J Finke, S V Medendorp, S Murthy, C Novak, J Sergi, R Tubbs.   

Abstract

Because recombinant interleukin 2 (rIL-2) and recombinant alpha-interferon (rIFN-alpha) exhibit synergistic antitumor activity in C3HMT1820 T-cell lymphoma and B16 melanoma tumor systems, we have performed a Phase I study of this combination in 55 patients with advanced malignancies for whom no standard therapy exists. Successive groups of greater than or equal to 4 patients have been entered into 12 dose levels (1A-3D), with dose levels 1-3 referring to doses of rIL-2 of 0.1, 0.5, and 2.0 x 10(6) units/m2, respectively, and dose levels A-D referring to doses of recombinant human alpha 2a-interferon (rHuIFN-alpha 2a) of 0, 0.1, 1.0, and 10.0 x 10(6) units/m2. Both agents were given on Mondays, Wednesdays, and Fridays, with rIL-2 being given as i.v. bolus injections and rHuIFN-alpha 2a being given intramuscularly. Myelosuppression was dose-limiting and was related primarily to the dose of rHuIFN-alpha 2a. The maximum-tolerated dose level was reached at a dose of rIL-2 of 2.0 x 10(6) units/m2 and of rHuIFN-alpha 2a of 10.0 x 10(6) units/m2 (dose level 3D). At this dose level, 3/6 patients developed grade 3 neutropenia (absolute granulocyte count less than 1 x 10(9)/liter). Myelosuppression was transient, with no documented infections being associated with neutropenia. Hypotension was mild; a single patient was treated with a vasopressor, but all other cases of hypotension responded to fluid administration. No significant pulmonary toxicity was produced. Fever, chills, and malaise were universal but not dose-limiting. Three partial responses and one minor response were observed in patients with malignant melanoma, renal cell carcinoma, and breast cancer. Immunological studies suggested that natural killer activity was related to both the dose of rIL-2 and the dose of rHuIFN-alpha 2a, with natural killer activity being positively related to the dose of rIL-2 and maximal at the lowest dose of rHuIFN-alpha 2a of 0.1 x 10(6) units/m2.

Entities:  

Mesh:

Substances:

Year:  1989        PMID: 2804986

Source DB:  PubMed          Journal:  Cancer Res        ISSN: 0008-5472            Impact factor:   12.701


  9 in total

Review 1.  Rationale for immunotherapy of renal cell carcinoma.

Authors:  R Heicappell; R Ackermann
Journal:  Urol Res       Date:  1990

2.  Order of administration of combination cytokine therapies can decouple toxicity from efficacy in syngeneic mouse tumor models.

Authors:  Adrienne Rothschilds; Alice Tzeng; Naveen K Mehta; Kelly D Moynihan; Darrell J Irvine; K Dane Wittrup
Journal:  Oncoimmunology       Date:  2019-02-19       Impact factor: 8.110

3.  Renal, metabolic, and hemodynamic side-effects of interleukin-2 and/or interferon alpha: evidence of a risk/benefit advantage of subcutaneous therapy.

Authors:  A Schomburg; H Kirchner; J Atzpodien
Journal:  J Cancer Res Clin Oncol       Date:  1993       Impact factor: 4.553

4.  Low-dose recombinant interleukin-2 and low-dose cyclophosphamide in metastatic breast cancer.

Authors:  D V Spicer; A Kelley; R Herman; G Dean; L Stevenson; M S Mitchell
Journal:  Cancer Immunol Immunother       Date:  1992       Impact factor: 6.968

Review 5.  Cytokine combinations in immunotherapy for solid tumors: a review.

Authors:  K M Heaton; E A Grimm
Journal:  Cancer Immunol Immunother       Date:  1993-09       Impact factor: 6.968

6.  Increased LAK and T cell activation in responding renal cell carcinoma patients after low dose cyclophosphamide, IL-2 and alpha-IFN.

Authors:  P Wersäll; H Mellstedt
Journal:  Med Oncol       Date:  1995-06       Impact factor: 3.064

7.  Subcutaneously administered recombinant human interleukin-2 and interferon alfa-2a for advanced breast cancer: a phase II study of the Cancer and Leukemia Group B (CALGB 9041).

Authors:  Gretchen Kimmick; Mark J Ratain; Don Berry; Susan Woolf; Larry Norton; Hyman B Muss
Journal:  Invest New Drugs       Date:  2004-01       Impact factor: 3.850

8.  Immunomodulation during prolonged treatment with combined interleukin-2 and interferon-alpha in patients with advanced malignancy.

Authors:  A von Rohr; A K Ghosh; N Thatcher; P L Stern
Journal:  Br J Cancer       Date:  1993-01       Impact factor: 7.640

9.  Final report of a phase II study of interleukin 2 and interferon alpha in patients with metastatic melanoma.

Authors:  W H Kruit; S H Goey; F Calabresi; A Lindemann; R A Stahel; H Poliwoda; B Osterwalder; G Stoter
Journal:  Br J Cancer       Date:  1995-06       Impact factor: 7.640

  9 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.